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Frontiers Case Report: Complete Maternal Uniparental Disomy of Chromosome 2 With a Novel UNC80 Splicing Variant c.5609-4G> A in a Chinese Patient With Infantile Hypotonia With Psychomotor Retardation and Characteristic Facies

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IJMS January 2017 - Browse Articles

vocab.txt · yihanlin/scibert_scivocab_uncased at main

IJMS January 2017 - Browse Articles

Genetic screens in Caenorhabditis elegans models for neurodegenerative diseases - ScienceDirect

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